916497-81-9

Upstream product

• 10022-13-6 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranose 
• 102231-96-9 p-octyloxybenzenethiol 
• 72858-55-0 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-D-glucopyranose 
• 21095-40-9 4-(octyloxy)benzene-1-sulfonyl chloride 

Downstream Products

• 1242660-03-2 3,4,6-tri-O-acetyl-2-N-phthaloyl-β(1-2)-D-glucosaminyl-3-O-benzyl-(4,6)-benzylidene-β-D-mannopyranosyl p-octyloxyphenyl sulfoxide 
• 1242660-00-9 3,4,6-tri-O-acetyl-2-N-phthaloyl-β(1-6)-D-glucosaminyl-2,3,4-tri-O-benzyl-β-D-glucopyranosyl p-octyloxyphenyl sulfoxide 
• 1010692-62-2 C₇₂H₈₁NO₂₀Si 

Relevant academic research and scientific papers

Glycosylation reaction of thioglycosides by using hypervalent iodine(III) reagent as an excellent promoter

Thioglycosides are available donors in glycosylation due to the stability of the anomeric C-S bond under general reaction conditions of protection and deprotection, and offer orthogonality in their activation. We report now that the hypervalent iodine eff

Phenyliodine bis(trifluoroacetate) (PIFA) as an excellent promoter of 2-deoxy-2-phthalimido-1-thioglycosides in the presence of triflic acid in glycosylation reactions

A combination of phenyliodine bis(trifluoroacetate) (PIFA) and trifluoromethanesulfonic acid was found to be an effective activator for the glycosylation reaction, of which the glycosyl donor was p-(octyloxy)phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido

Odorless benzenethiols in synthesis of thioglycosides and its application for glycosylation reactions

p-Octyloxybenzenethiol (2) was synthesized as a new odorless benzenethiol. Moreover, preparation of thioglycosides using 2 and their application for glycosylation reactions were attempted. As a result, it was found that the thioglycosides were as excellen